Zhang Junfeng
Department of Health Statistics / the Publishing house, Public Health of Shanxi Medical University / Chinese Journal of Rheumatology, Taiyuan, Shanxi, 030001, China.
BMC Musculoskelet Disord. 2018 Jan 19;19(1):22. doi: 10.1186/s12891-018-1932-y.
The roles of C-reactive protein (CRP) and cartilage oligomeric matrix protein (COMP) in knee osteoarthritis (KOA) remain controversial, thus the present study is aimed to explore the relationships between CRP, COMP, and the incidence/progression of KOA.
A systematic search was conducted on PubMed and Embase until September, 2016 for all the relevant studies. The pooled mean difference (MD) with its 95% confidence interval (95% CI) based on fixed effects model or random effects model was calculated to assess the potential role of CRP and COMP in the incidence or progression of KOA. Heterogeneity was evaluated by Cochran's Q and I tests. When P < 0.05 or I > 50%, a random effects model was chosen, otherwise, a fixed effects model was used. Moreover, the role of CRP in different degrees of pain was also analyzed. Sensitivity analysis was performed to evaluate the strength of the meta-analysis.
Fourteen studies were enrolled in the meta-analysis. No difference was found between baseline CRP and CRP levels in the last follow-up period of KOA (MD = - 0.09, 95% CI: -0.30, 0.13). Pooled data showed higher CRP concentration in patients with incident KOA when compared with controls (MD = 0.33, 95% CI: 0.04, 0.63). Moreover, higher serum COMP levels were found in patients with incident KOA (MD = 1.69, 95% CI: 0.61, 2.76) Additionally, significant higher CRP concentration was observed in KOA patients with highest degree of pain (MD = 1.60, 95% CI: 0.52, 2.67).
CRP and COMP serum levels were both associated with the incidence of KOA. Patients with a higher CRP and COMP concentration might have an increased probability of developing KOA. However, higher CRP serum levels was not related with KOA progression. Furthermore, KOA patients with more pain had higher CRP concentrations.
C反应蛋白(CRP)和软骨寡聚基质蛋白(COMP)在膝关节骨关节炎(KOA)中的作用仍存在争议,因此本研究旨在探讨CRP、COMP与KOA发病率/进展之间的关系。
截至2016年9月,在PubMed和Embase上对所有相关研究进行系统检索。基于固定效应模型或随机效应模型计算合并平均差(MD)及其95%置信区间(95%CI),以评估CRP和COMP在KOA发病率或进展中的潜在作用。通过Cochran's Q检验和I²检验评估异质性。当P<0.05或I²>50%时,选择随机效应模型,否则使用固定效应模型。此外,还分析了CRP在不同程度疼痛中的作用。进行敏感性分析以评估荟萃分析的强度。
14项研究纳入荟萃分析。KOA最后随访期的基线CRP与CRP水平之间未发现差异(MD = -0.09,95%CI:-0.30,0.13)。汇总数据显示,与对照组相比,新发KOA患者的CRP浓度更高(MD = 0.33,95%CI:0.04,0.63)。此外,新发KOA患者的血清COMP水平更高(MD = 1.69,95%CI:0.61,2.76)。另外,在疼痛程度最高的KOA患者中观察到CRP浓度显著更高(MD = 1.60,95%CI:0.52,2.67)。
CRP和COMP血清水平均与KOA的发病率相关。CRP和COMP浓度较高的患者发生KOA的可能性可能增加。然而,较高的CRP血清水平与KOA进展无关。此外,疼痛更严重的KOA患者CRP浓度更高。